Active Ingredient
Ethyl alcohol 70%
Konix Hand Sanitizer Gel
FDA Label NDC 73107-106
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal Urunler Sanayi Ve Tic. As for the product Konix Hand Sanitizer Gel (NDC 73107-106). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, use, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic, Hand Sanitizer Gel
Use
To decrease bacteria on the skin that could cause disease
Warnings
For external use only: hands.
Flammable, keep away from fire or flame.
Otc - When Using
When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water. avoid contact with broken skin do not inhale or ingest
Otc - Stop Use
Stop use and ask a doctor if Irritation and redness develop Condition persists for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
wet hands thoroughly with product and allow to dry without wiping
for children under 6 year of age, use only under adult supervision
Not recommended for infants
Other Information
do not store above 105°F
may discolor some fabrics
harmful to wood finishes and plastics
Inactive Ingredients
Water, Glycerin, Carbomer, Fragrance, Aminomethyl Propanol
* Please review the disclaimer below.
